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Analysis of the internal or mechanical cues to regulate planar polarity for the neural tube formation

Research Project

Project/Area Number 17K07427
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Developmental biology
Research InstitutionNara Institute of Science and Technology

Principal Investigator

Nishimura Tamako  奈良先端科学技術大学院大学, 先端科学技術研究科, 助教 (40415261)

Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2019: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2018: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
KeywordsCelsr1 / neural tube / Wnt / I-BAR / BARタンパク質 / PCP / planar polarity
Outline of Final Research Achievements

When the neuroepithelial layer is invaginated during the neural tube closure, a planar polarity protein Celsr1 is distributed to the cell-cell contacts along the dorsoventral axis and contracts actin filaments in that direction. However, upstream signals that polarize Celsr1 are unknown.
Therefore, we investigated the possibility that mechanical stimuli added to cells or internal stimuli such as Wnt might be involved in the process. As a result, some of the Wnt molecules were secreted through microvesicles, which are extracellular vesicles derived from the plasma membrane, and activated the Wnt receptor. Furthermore, I-BAR proteins, which deform and cleave the plasma membrane, were found to be involved in the Wnt secretion.
We would like to elucidate next whether these phenomena are involved in the polar-polarized distribution of Celsr1.

Academic Significance and Societal Importance of the Research Achievements

内的刺激因子Wntは、これまでタンパク質複合体やエンドソーム系細胞外小胞エクソソームを介して分泌されると考えられており、細胞突起由来のマイクロベシクルを介して分泌されうることを示したのは我々が初めてである。I-BARタンパク質MIMは神経管形成への関与が報告されており、その作用がCelsr1の極性分布を介する可能性がある。神経管の異常形成は新生児の先天性疾患で2番目に多く、Celsr1の様々な変異が報告されている。Celsr1を介したシグナル伝達の解明により、異常の原因解明や予防・治療につながる可能性がある。

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (17 results)

All 2019 2018 2017

All Journal Article (5 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 3 results,  Open Access: 2 results) Presentation (12 results) (of which Int'l Joint Research: 2 results,  Invited: 2 results)

  • [Journal Article] Phagocytosis is mediated by two-dimensional assemblies of the F-BAR protein GAS72019

    • Author(s)
      Hanawa-Suetsugu Kyoko et al.
    • Journal Title

      Nature Communications

      Volume: 10 Issue: 1 Pages: 4763-4763

    • DOI

      10.1038/s41467-019-12738-w

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] BARドメインタンパク質と細胞骨格による細胞膜の構造構築2018

    • Author(s)
      西村 珠子、末次 志郎
    • Journal Title

      生体の科学

      Volume: 69 Pages: 203-207

    • Related Report
      2018 Research-status Report
  • [Journal Article] Membrane re-modelling by BAR domain superfamily proteins via molecular and non-molecular factors.2018

    • Author(s)
      Tamako Nishimura, Nobuhiro Morone and Shiro Suetsugu
    • Journal Title

      Biochemical Society Transactions

      Volume: 46 Issue: 2 Pages: 379-389

    • DOI

      10.1042/bst20170322

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] BARドメインタンパク質と細胞骨格による細胞膜の構造構築2018

    • Author(s)
      西村珠子、末次志郎
    • Journal Title

      生体の科学

      Volume: 69 Pages: 1-5

    • Related Report
      2017 Research-status Report
  • [Journal Article] Induced cortical tension restores functional junctions in adhesion-defective carcinoma cells.2017

    • Author(s)
      Shoko Ito, Satoru Okuda, Masako Abe, Mari Fujimoto, Tetsuo Onuki, Tamako Nishimura and Masatoshi Takeichi
    • Journal Title

      Nature Communications

      Volume: 8 Issue: 1 Pages: 1834-1834

    • DOI

      10.1038/s41467-017-01945-y

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] Wntのマイクロベシクル局在におけるI-BARドメインタンパク質の役割2019

    • Author(s)
      中村 暢明、西村 珠子、末次 志郎
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] I-BARタンパク質MIMを介したマイクロベシクルの形成機序2019

    • Author(s)
      西村珠子、大山 拓也、Hu Hooi Ting、塙 京子、末次 志郎
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] 細胞生物学研究者による細胞生物学におけるデータサイエンスの試み2019

    • Author(s)
      末次 志郎、西村 珠子、重根 桂、日朝 祐太、大竹 義人、佐藤 嘉伸
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
    • Invited
  • [Presentation] 細胞突起形成タンパク質IRSp53のドメイン依存的な分泌制御2019

    • Author(s)
      高橋 茉奈美、西村 珠子、塙 京子、末次 志郎
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] The interaction between I-BAR domain proteins and ALIX in the formation and release of extracellular vesicles2019

    • Author(s)
      Hooi Ting Hu、Tamako Nishimura、Shiro Suetsugu
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] 機械学習を用いたタンパク質局在に基づく細胞形態の記述の試み2019

    • Author(s)
      重根 桂、西村 珠子、日朝 祐太、大竹 義人、佐藤 嘉伸、末次 志郎
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] Development of the Green Photoswitchable Fluorescent Protein with Fixation Resistance, a Variant of Eos Fluorescent Protein.2019

    • Author(s)
      Mitsuo Osuga, Tamako Nishimura, Shiro Suetsugu
    • Organizer
      ASCB/EMSO 2019 meeting
    • Related Report
      2019 Annual Research Report
    • Int'l Joint Research
  • [Presentation] In-vitro FRET Analysis of Growth Arrest-Specific Protein 7 (GAS7).2019

    • Author(s)
      Wan Nurul Izzati Wan Mohamad Noor, Tamako Nishimura, Shiro Suetsugu
    • Organizer
      ASCB/EMSO 2019 meeting
    • Related Report
      2019 Annual Research Report
    • Int'l Joint Research
  • [Presentation] I-BARタンパク質MIMによる細胞膜切断を介したマイクロベシクル形成機構2019

    • Author(s)
      西村珠子、末次志郎
    • Organizer
      第92回日本生化学会年大会
    • Related Report
      2019 Annual Research Report
    • Invited
  • [Presentation] I-BARドメインタンパク質IRTKSの細胞間接着における役割2018

    • Author(s)
      西村珠子、末次志郎
    • Organizer
      第41回日本分子生物学会年会
    • Related Report
      2018 Research-status Report
  • [Presentation] 固定耐性を持つ点滅蛍光タンパク質の開発の試み2018

    • Author(s)
      大菅光雄、西村珠子、末次志郎
    • Organizer
      第41回日本分子生物学会年会
    • Related Report
      2018 Research-status Report
  • [Presentation] 固定耐性を持つ点滅可能蛍光タンパク質の開発2018

    • Author(s)
      大菅光雄、西村珠子、末次志郎
    • Organizer
      科学研究費補助金・新学術領域「数理シグナル」第二回公開シンポジウム「数理シグナル 学術領域の新展開」
    • Related Report
      2017 Research-status Report

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Published: 2017-04-28   Modified: 2023-01-30  

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